RUBY Coil - Indonesia BPOM Medical Device Registration
RUBY Coil is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003913248. The device is manufactured by PENUMBRA INC. from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. BISAWI GROWS IN HARMONY.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
PENUMBRA INC.Country of Origin
United States
Authorized Representative
PT. BISAWI GROWS IN HARMONYAR Address
Graha Kencana Blok EU Jl. Raya Perjuangan No.88 Kebun Jeruk Jakarta Barat
Registration Date
Nov 18, 2023
Expiry Date
Dec 31, 2026
Product Type
Therapeutic Neurology Equipment
Neurovascular embolization device.
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